CAS:128376-64-7 | 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

Properties:

1. Physical properties: 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a colorless to pale yellow powder, insoluble in water at room temperature organic solvent.
2. Chemical properties: it is an aromatic compound with ester group, which can occur esterification reaction, oxidation reaction, etc. The chemical properties of the compound determine its use in laboratory and industry.
3. Its CAS number is 128376-64-7, its chemical formula is C₁₃H₁₇BO₃, and its molecular weight is 232.08. Its density is estimated to be 1.06±0.1 g/cm3, its melting point is 55-58°C, and its boiling point is estimated to be 341.3±25.0°C. Its flash point is 160.2°C, and it is slightly soluble in water. Its vapor pressure at 25°C is 8.11×10⁻⁵mmHg, and its refractive index is 1.501. It should be stored in a dark, sealed, dry place at room temperature.

Uses:

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is an important organic synthesis intermediate with a wide range of uses in medicine, materials science and other fields:

• Medicine: It can be used to synthesize a variety of biologically active compounds and is a key intermediate for the preparation of some drugs for the treatment of cardiovascular diseases and nervous system diseases. In medicinal chemistry, this compound can be used to modify the structure of existing drug molecules to improve the physicochemical properties and pharmacokinetic properties of drugs.
• Materials science: It is an important raw material for the preparation of organic materials with photoelectric properties. It can be used for functional modification of material surfaces, connecting it to the material surface through chemical reactions, thereby changing the chemical properties and physical properties of the material surface. It has potential applications in the fields of biomedical materials and sensors.
• Organic synthesis: In organic synthesis reactions, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde can be used as an arylation agent to react with various electrophiles or nucleophiles to construct new carbon-carbon bonds and carbon-hetero bonds, providing an effective method for synthesizing complex organic molecules. It can participate in various types of organic reactions and is widely used in the fields of total synthesis of natural products, drug synthesis, and preparation of functional organic molecules.

Safety Information：

In case of accidental contact with eyes, rinse immediately with plenty of water and seek medical advice.
Wear appropriate protective clothing, gloves and goggles or mask.
Wear appropriate protective clothing and gloves.

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